CRC 102 - Clinical Research Coordination II

This course explores core competency domains and examines a variety of subjects including the processes and essential components of a protocol in depth, elements of informed consent, and the types, roles, jurisdiction and submission requirements for Institutional Review Board review. This course will also teach important skills for a good coordinator, including how to build a compliant regulatory binder; how to maintain master trial files, electronic and paper binders; and understanding source documentation. In addition, students will complete the Human Subjects Protection training, CITI, and Good Clinical Practice and be certified in the same. This class is only open to students in the CRC certificate program.

Prerequisite(s): CRC 101, CRC 131, ENG 111